FDA Voices (2026): MoCRA implementation progress — treat as a status board
FDA’s May 2026 Voices post walks listing, PFAS report, and leftover rulemakings. Useful as a checklist against the MoCRA statute page.
FDA’s May 2026 Voices post walks listing, PFAS report, and leftover rulemakings. Useful as a checklist against the MoCRA statute page.
An SCCS opinion is scientific advice to the Commission. It is not an annex amendment. Triage: listed in CosIng annex already, or still only an opinion?
The Commission’s allergen topic page is context. The binding table is Annex III as amended by 2023/1545.
ACSB annex updates only become “your problem” when a Member State issues a circular. Budget ten front doors, not one ASEAN certificate.
FDA’s MoCRA-mandated PFAS report found evidence too thin for safety determinations on most intentionally added PFAS. State bans can still apply.
NMPA told provincial regulators to run a three-year quality-system improvement action. Manufacturers in China should expect deeper file-vs-floor checks.
“Salon only” is not a MoCRA off-ramp. Adverse-event contact and other required statements still need a home on the pack or the mandated alternative.
NMPA’s 24-measure reform opinion sets a 2030 destination. Use it to understand why 2026 announcements exist — do not file against a white paper.
Article 4 and Article 13 duties did not change in 2025. They still cause more failed first shipments than annex chemistry.
Statutory target dates for some MoCRA rules have slipped. Track FDA’s MoCRA page. Do not implement a draft you cannot cite.